Autosomal dominant distal myopathy with nemaline rods due to p.Glu197Asp mutation in ACTA1

  1. Hernandez-Lain, A.
  2. Cantero, D.
  3. Camacho-Salas, A.
  4. Toldos, O.
  5. Esteban, I.
  6. Pascual, I.
  7. Dominguez-Gonzalez, C.
Aldizkaria:
Neuromuscular Disorders

ISSN: 1873-2364 0960-8966

Argitalpen urtea: 2019

Alea: 29

Zenbakia: 3

Orrialdeak: 247-250

Mota: Artikulua

DOI: 10.1016/J.NMD.2018.12.001 GOOGLE SCHOLAR